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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 569377생성일: 2026년 10월 26일

Phosphorus oxychloride → Benzhydryl 7-[4-bromo-2-(2,2,2-trichloroethoxycarbonylmethoxyimino)-3-oxobutyramido]-3-vinyl-3-cephem-4-carboxylate

https://huagongshe.com/reaction/569377

반응식

참여 물질

역할이름HCID투입량
반응물Phosphorus oxychlorideHCID 24813—
반응물Chloro-N,N-dimethylformiminium chlorideHCID 77311—
반응물Acetamide, 2-(trimethylsilyl)-HCID 357676—
반응물Benzhydryl 7-amino-3vinyl-3cephem-4-carboxylate hydrochlorideHCID 12818005—
반응물4-Bromo-2-(2,2,2-trichloroethoxycarbonylmethoxyimino)-3-oxobutyric acidHCID 53866482—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물Benzhydryl 7-[4-bromo-2-(2,2,2-trichloroethoxycarbonylmethoxyimino)-3-oxobutyramido]-3-vinyl-3-cephem-4-carboxylateHCID 13171333489%

반응 조건

온도5 °C

반응 단계

Vilsmeier reagent prepared from phosphorus oxychloride (7.1 ml) and N,N-dimethylformamide (6.0 ml) was suspended in dry tetrahydrofuran (25 ml). To this suspension was added 4-bromo-2-(2,2,2-trichloroethoxycarbonylmethoxyimino)-3-oxobutyric acid (25 g), and the mixture was stirred at 5° C. for an hour to prepare the activated acid solution. This solution was added at a time to a solution of benzhydryl 7-amino-3-vinyl-3-cephem-4-carboxylate hydrochloride (16.2 g) and trimethylsilylacetamide (40 g) in ethyl acetate (140 ml) at -30° C., and the mixture was stirred at -15° to -5° C. for an hour. The reaction mixture was extracted with ethyl acetate, and the extract was washed with a saturated aqueous sodium bicarbonate and a saturated aqueous sodium chloride, followed by drying over magnesium sulfate. Removal of the solvent gave benzhydryl 7-[4-bromo-2-(2,2,2-trichloroethoxycarbonylmethoxyimino)-3-oxobutyramido]-3-vinyl-3-cephem-4-carboxylate (26.0 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04731443
출처 데이터셋uspto-grants-1988_03
ORD IDord-4608693ceca74119b70f4a4e6f2c0be3
출처 메모uspto-grants-1988_03